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Clinical research Training clinical data management Course with SAS and Imaging by Clinnovo

Clinical Research Services

    • We manage simple and complex clinical trials.
    • Complete responsibility of clinical Data management process for multiple clinical trials.
    • Data analysis and reporting.
    • Database quality checks and data validation.
    • Data Analysis, Data Mining & Secondary Research.
    • Acquisition of data from internet, Case Report Forms (CRFs) & Data Clarification Forms (DCFs)

    Back office & Data curation

    • Collect & analyze the information about marketed & development stage products of Pharmaceutical companies including clinical trial data, regulatory information (approvals & filings of NDA, BLA etc), press release tracking & analysis, Deal-M&A (mergers & acquisitions), patent updates capture for products & companies from various secondary sources like company websites, regulatory sites, Clinicaltrials.gov, SEC filings, annual reports, scientific journals, healthcare conferences and annual meetings like ASCO, ASH, SABCS etc.
    • Wide variety of public & proprietary data bases: FDA, EMEA, ClinicalTrials.gov, NCI, CTRI, UMIN, Medscape, PubMed, Science Direct etc for trial related information of patients like patient segment, therapeutic area, target accrual, actual accrual, status of a trial, study design, inclusion and exclusion criteria, information of investigators involved etc.
    • Construct records for clinical trials conducted all over the world and extract out information from various therapeutic areas’ annual meetings, journals, company registries, company press releases and countries registries.
    • Data entry of Phase II-IV clinical trials.
    • Perform web search of various clinical trials on various criteria that we follow in our work-process and assemble the data thoroughly and with high precision.
    • Manage your content writing, literature, social media.